Utilization and evaluation of CHO‐specific sequence databases for mass spectrometry based proteomics

Paula Meleady(Dublin City University), Raimund Hoffrogge(Bielefeld University), Michael Henry(Dublin City University), Oliver Rupp(Bielefeld University), Juan A. Hernández Bort(Austrian Centre of Industrial Biotechnology (Austria)), Colin Clarke(Dublin City University), Karina Brinkrolf(Bielefeld University), Shane Kelly(Dublin City University), Benjamin Müller(GTx (United States)), Padraig Doolan(Dublin City University), Matthias Hackl(BOKU University), Tim Beckmann(GTx (United States)), Thomas Noll(GTx (United States)), Johannes Grillari(BOKU University), Niall Barron(Dublin City University), Alfred Pühler(Bielefeld University), Martin Clynes(Dublin City University), Nicole Borth(Bielefeld University)
Biotechnology and Bioengineering
February 21, 2012
Cited by 55

Abstract

Recently released sequence information on Chinese hamster ovary (CHO) cells promises to not only facilitate our understanding of these industrially important cell factories through direct analysis of the sequence, but also to enhance existing methodologies and allow new tools to be developed. In this article we demonstrate the utilization of CHO specific sequence information to improve mass spectrometry (MS) based proteomic identification. The use of various CHO specific databases enabled the identification of 282 additional proteins, thus increasing the total number of identified proteins by 40-50%, depending on the sample source and methods used. In addition, a considerable portion of those proteins that were identified previously based on inter-species sequence homology were now identified by a larger number of peptides matched, thus increasing the confidence of identification. The new sequence information offers improved interpretation of proteomic analyses and will, in the years to come, prove vital to unraveling the CHO proteome.


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